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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A0A2R8Y535 ATP2B2 ATPase plasma membrane Ca2+ transporting … Homo sapiens (Human) 387 aa

Protein Details: A0A2R8Y535 (ATP2B2)

Protein Information
Accession A0A2R8Y535
Protein Names ATPase plasma membrane Ca2+ transporting 2
Gene Symbol ATP2B2
Organism Homo sapiens (Human)
Length 387 aa
Isoforms No isoforms
Related PMIDs 26876311
Database Sources No database sources
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
1
Prefrontal cortex
Specificity: 1.000
1/1 (100.0%)
0
Jurkat T cells
Specificity: 0.000
0/25 (0.0%)
0
U937 cells
Specificity: 0.000
0/1 (0.0%)
0
DU145 cells
Specificity: 0.000
0/2 (0.0%)
0
HeLa cells
Specificity: 0.000
0/1 (0.0%)
0
LNCaP cells
Specificity: 0.000
0/46 (0.0%)
0
PC3 cells
Specificity: 0.000
0/4 (0.0%)
0
T cells
Specificity: 0.000
0/4 (0.0%)
0
HAP1 cells
Specificity: 0.000
0/10 (0.0%)
0
293T cells
Specificity: 0.000
0/10 (0.0%)
0
CEMx174 cells
Specificity: 0.000
0/3 (0.0%)
0
Endothelial cells
Specificity: 0.000
0/2 (0.0%)
0
Cerebral cortex
Specificity: 0.000
0/4 (0.0%)
0
Liver membrane
Specificity: 0.000
0/1 (0.0%)
Palmitoylation Distribution by Study and Tissue/Cell Line
Chart Explanation: Each bar represents a study (PMID). The colored bottom segment shows palmitoylated samples, while the gray top segment shows non-palmitoylated samples. Bars are grouped by tissue/cell line for easy comparison.
Protein Sequence
Single Types:
Experimental Database High Prediction Medium Prediction Low Prediction
Combined Types:
All Three Exp + DB Exp + High Pred Exp + Med Pred Exp + Low Pred DB + High Pred DB + Med Pred DB + Low Pred Cysteine
1-501GPALKKADVG11FAMGIAGTDV21AKEASDIILT31DDNFSSIVKA41VMWGRNVYDS
51-10051ISKFLQFQLT61VNVVAVIVAF71TGACITQDSP81LKAVQMLWVN91LIMDTFASLA
101-150101LATEPPTETL111LLRKPYGRNK121PLISRTMMKN131ILGHAVYQLA141LIFTLLFVGE
151-200151KMFQIDSGRN161APLHSPPSEH171YTIIFNTFVM181MQLFNEINAR191KIHGERNVFD
201-250201GIFRNPIFCT211IVLGTFAIQI221VIVQFGGKPF231SCSPLQLDQW241MWCIFIGLGE
251-300251LVWGQSRIGC261LQGPVTSGGI271RDRGISNPRR281TEGQPRARLM291QDELDPPPCP
301-350301VLTMPRAAPT311LQLGKPKLGH321RHHPDQQTQV331PQGGRQAHTE341GGDPGGGAQR
351-387351GRGGDRPRGA361GAAAGPDPVV371PRPESDPDTD381PRREGVP
Palmitoylation Sites Details
Position Sources Domains Experimental PMIDs
74 Prediction (Medium) - -
232 Prediction (Medium) - -
260 Prediction (Low) - -
Conservation Scores
PhyloP
PhastCons
TCGA Cysteine Mutation Information

Note: Mutations indicate amino acid changes that may create potential palmitoylation sites.

Position Amino Acid Change Frequency Type Function Cancer Type
32 R → C 0.002141 SNP Missense Mutation SKCM
32 R → C 0.001887 SNP Missense Mutation UCEC
59 R → C 0.002294 SNP Missense Mutation OV
86 F → C 0.007299 SNP Missense Mutation READ
151 W → C 0.001887 SNP Missense Mutation UCEC
185 R → C 0.001764 SNP Missense Mutation LUAD
249 R → C 0.002288 SNP Missense Mutation STAD
249 R → C 0.002506 SNP Missense Mutation COAD
432 C → S 0.006944 SNP Missense Mutation TGCT
491 G → C 0.002033 SNP Missense Mutation LUSC
497 C → S 0.001764 SNP Missense Mutation LUAD
559 G → C 0.002288 SNP Missense Mutation STAD
588 R → C 0.001887 SNP Missense Mutation UCEC
597 Y → C 0.001887 SNP Missense Mutation UCEC
606 R → C 0.001969 SNP Missense Mutation HNSC
606 R → C 0.002020 SNP Missense Mutation PRAD
606 R → C 0.001887 SNP Missense Mutation UCEC
621 R → C 0.001764 SNP Missense Mutation LUAD
621 R → C 0.002141 SNP Missense Mutation SKCM
651 R → C 0.001887 SNP Missense Mutation UCEC
666 C → C 0.001887 SNP Silent UCEC
673 C → C 0.001887 SNP Silent UCEC
677 R → C 0.005435 SNP Missense Mutation ESCA
699 C → C 0.001887 SNP Silent UCEC
869 R → C 0.001887 SNP Missense Mutation UCEC
1014 R → C 0.001887 SNP Missense Mutation UCEC
1020 R → C 0.001887 SNP Missense Mutation UCEC
1055 S → C 0.002747 SNP Missense Mutation LIHC
1067 C → C 0.003460 SNP Silent CESC
1142 R → C 0.002141 SNP Missense Mutation SKCM
1178 S → C 0.002294 SNP Missense Mutation OV
1211 S → C 0.001764 SNP Missense Mutation LUAD